A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088516



Internal ID15941702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78505547..78519663hg38UCSC Ensembl
Innerchr7:78134864..78148980hg19UCSC Ensembl
Innerchr7:77972800..77986916hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3814117
hg1914117
hg1814117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607655
Supporting Variants
Samples
Known GenesMAGI2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1088516
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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